US20130190537A1

US20130190537A1 - Heterogeneous catalysts

Info

Publication number: US20130190537A1
Application number: US13/825,610
Authority: US
Inventors: Palanichamy Manikandan; Sreenivasa Rao; Phani Kiran Bollapragada
Original assignee: Dow Global Technologies LLC
Current assignee: Dow Global Technologies LLC
Priority date: 2010-10-11
Filing date: 2011-09-26
Publication date: 2013-07-25
Anticipated expiration: 2031-09-26
Also published as: BR112013007281A2; CN103261127A; WO2012050807A1; US8766014B2; EP2627619A1; CN103261127B; EP2627619B1

Abstract

Convert a mixture of synthesis gas and ethylene to a product stream that contains at least one C3 oxygenate using a supported, heterogeneous catalyst represented by formula Rh_aAg_bSn_cX_dY_eO_x. In the formula, X is at least one transition element other than rhodium or silver, and Y is at least one element selected from alkali metals and alkaline earth metals.

Description

This application is a non-provisional application claiming priority from the U.S. Provisional Patent Application No. 61/391,742, filed on Oct. 11, 2010, entitled “HETEROGENEOUS CATALYSTS” the teachings of which are incorporated by reference herein, as if reproduced in full hereinbelow.
This invention relates to a process for converting a feedstream of ethylene and synthesis gas (“syngas”, a mixture of carbon monoxide (CO) and hydrogen (H₂)) to a product stream that comprises at least one three carbon (C₃) oxygenate (e.g. propionaldehyde or propanol) using a heterogeneous catalyst that comprises a combination of metals on a catalyst support.
Steven S. C. Chuang et al., in “Role of Silver Promoter in Carbon Monoxide Hydrogenation and Ethylene Hydroformylation over Rh/SiO₂Catalysts”, Journal of Catalysis, 138, 536-546 (1992), teach that silver (Ag) increases selectivity and rate of formation for acetaldehyde (a two carbon atom (C₂) oxygenate) during CO hydrogenation and for propionaldehyde during ethylene hydroformylation on a silica (SiO₂)-supported rhodium (Rh) catalyst. They also teach that certain promoters, such as manganese (Mn), zirconium (Zr), titanium (Ti), vanadium (V) and lanthanum (La) oxides as well as alkali metals, are known to enhance C₂oxygenate selectivity, while other promoters, including zinc (Zn) and iron (Fe), modify catalyst activity by blocking surface sites.
Steven S. C. Chuang et al., in “C₂Oxygenate Synthesis from CO Hydrogenation on AgRh/SiO₂ ”, Applied Catalysis, volume 57, pages 241-251, notes that Ag decreases rates of formation for methane and C₂₊hydrocarbons more than those for C₂oxygenates, resulting in a marked increase in C₂oxygenate selectivity.
U.S. Pat. No. 4,492,773 (Ball et al.) teaches production of C₁to C₄oxygenates by contacting syngas at a temperature within a range of 150 degrees Celsius (° C.) to 450° C. and a pressure within a range of from 1 bar (100 kilopascals (KPa) to 700 bars (70,000 KPa) with a catalyst comprising a supported mixture of a Rh component and an Ag component. Other metal components that may be incorporated include iron (Fe), Mn, Mo, tungsten (W), ruthenium (Ru), chromium (Cr), thorium (Th) and zirconium (Zr). Support materials include silica, alumina, silica/alumina, magnesia, thoria, titania, chromia, zirconia, and active carbon. The catalyst support may be activated with one or more metal or non-metal activator components selected from alkali metals, Th, Mn, Rh, Fe, Cr, Mo, Zr, rhenium (Re), Ag, boron (B) and phosphorous (P).
In some aspects, this invention is a process for converting a feedstream comprising syngas and ethylene to a product stream that comprises at least one three carbon oxygenate, which process comprises placing the feedstream in contact with a heterogeneous catalyst under conditions sufficient to effect conversion of the feedstream to the product stream, the catalyst comprising a combination of metals on a catalyst support, the combination of metals being represented by general formula Rh_aAg_bSn_cX_dY_eO_xwherein X is at least one transition element other than rhodium or silver, Y is at least one element selected from alkali metals and alkaline earth metals, a is a real number within a range of from 0 1 millimoles per hectogram (mmol/hg) to 50 mmol/hg, b is a real number within a range of from 0.1 mmol/hg to 50 mmol/hg, c is a real number within a range of from 0.1 mmol/hg to 50 mmol/hg, d is a real number within a range of from 0 mmol/hg to 250 mmol/hg, e is a real number within a range of from 0 mmol/hg to 1500 mmol/hg, and x is a real number greater than zero needed to balance the total charges of Rh, Ag, Sn, X and Y elements, the catalyst support being at least one of silica, alumina, titania, magnesia, magnesium aluminate, and zinc aluminate.
The combination of metals represented by the above general formula comprises, consists essentially of, or consists of Rh, Ag, and tin (Sn), optionally in further combination with at least one promoter selected from X (at least one transition metal other than silver or rhodium) when d is greater than 0 and Y (at least one alkali metal or alkaline earth metal) when e is greater than 0. When d, e or both d and e are 0, the corresponding element (X for d and Y for e) is absent from the combination of metals.
The process conditions for conversion of the feedstream to the product stream include at least one of a pressure within a range of from 12 pounds per square inch gauge (psig) (82.7 kilopascals (KPa)) to 4,000 psig (27.6 megapascals (MPa)), preferably from 20 bars (2 MPa) to 45 bar (4.5 MPa), a temperature of from 100° C. to 450° C., preferably from 280° C. to 320° C., a gas hourly space velocity (GHSV) within a range of from 25 reciprocal hours (h⁻¹) to 25,000 h⁻¹, preferably from 2000 h⁻¹to 10000 h⁻¹, and a feedstream ratio of ethylene to carbon monoxide to hydrogen (C₂H₄:CO:H₂) within a range of from 0.01:10:10 to 10.0:0.01:0.01, with a ratio of 1:1:1 yielding very satisfactory results.
The transition metals other than Rh and Ag are selected from a group consisting of elements 21 through 29 (scandium (Sc) through Cu, elements 39 (yttrium (Y) through 44 (ruthenium (Ru)), 46 (palladium (Pd), 57 through 79 (lanthanum (La) through Au) and all known elements from 89 (actinium (Ac) on as such elements are listed in The Periodic Table of the Elements (inside cover of Hawley' s Condensed Chemical Dictionary, Twelfth Edition (1993)). Preferred transition metals include Zn, Fe, Cr, Co, and Ir.
The alkali metals include sodium (Na), lithium (Li), potassium (K), rubidium (Rb), cesium (Cs) and francium (Fr). The alkaline earth metals include magnesium (Mg), beryllium (Be), calcium (Ca), strontium (Sr), barium (Ba) and radium (Ra). When the catalyst includes component Y, one may use at least alkali metal, or at least one alkaline earth metal or a combination of at least one alkali metal and at least one alkaline earth metal.
The catalyst support is at least one of silica, alumina, titania, magnesia, magnesium aluminate, magnesium-modified silica, magnesium-modified alumina, zirconium-modified silica, zirconium-modified alumna, zinc-modified silica, zinc-modified alumina, and zinc aluminate, with silica, magnesia, magnesium aluminate and alumina being preferred supports.
As an additional option, one may admix an alkali metal carbonate such as sodium carbonate with catalyst compositions represented by the above general formula.
The alkali metal carbonate appears to reduce catalyst acidity, a possible explanation for a reduced tendency to promote hydrogenation of alkenes to alkenes during the process of at least some aspects of this invention.
The process of at least some aspects of this invention has utility in producing at least one C₃oxygenate. The C₃oxygenates, in turn have utility in serving as feedstocks for production of other chemicals such as production of propylene by dehydration of propanol. Propylene, in turn, has utility as a feedstock in making a variety of polymeric materials such as polypropylene that finds a number of uses in fabricated articles.
The heterogeneous catalysts provide an ethylene conversion of more than 90 mole percent (mol %), based upon total moles of ethylene in the feedstream, and a selectivity to C₃oxygenates, preferably to propanol and propanal (propionaldehyde) of at least 70 mol % based upon total moles of product in the product stream. Selectivity to C₃oxygenates preferably favors propanol over propanal such that the product stream contains more propanol than propanal.
The heterogeneous catalysts represented by general formula Rh_aAg_bSn_cX_dY_eO_xhave a Rh content that is within a range of from 0 1 mmol/hg to 50 mmol/hg, preferably from 5 mmol/hg to 30 mmol/hg, an Ag content that is within a range of from 0.1 mmol/hg to 50 mmol/hg, preferably from 2 mmol/hg to 10 mmol/hg, a Sn content that is within a range of from 0.1 mmol/hg to 50 mmol/hg, preferably from 0 8 mmol/hg to 5 mmol/hg, an X content that is within a range of from 0 mmol/hg to 222 mmol/hg, preferably from 1 mmol/hg to 40 mmol/hg, a Y content that is within a range of from 0 mmol/hg to 1500 mmol/hg, preferably from 1 mmol/hg to 500 mmol/hg, and an O content is decided by the net compound formed. Each mmol/hg is based upon combined weight of Rh, Ag, Sn, X, Y and O.
Arabic numerals designate Examples (Ex) of the present invention and capital alphabetic letters indicate Comparative Examples (Comp Ex or CEx).

68839 EXAMPLES

CEx A

In a 10 ml glass vial, add an aqueous solution (0.95 ml) containing 48.59 micromoles mol) (10.17 mg) RhCl₃·3 H₂O to 0.5 g of silica (Davison™57, surface area=280±20 m²/g) and stir the resultant mixture with a metal whisk at room temperature. Subject container contents to drying overnight at 120° C. (under vacuum?) Impregnate the dried contents with 0.475 ml of an aqueous solution containing 21.75 (μmol) (1.27 mg) NaCl. Dry the impregnated contents at room temperature for 4 hrs. Calcine dried container contents in air at 400° C. for 4 hrs in static air (heating rate of 2° C/minute) to yield a catalyst represented as Rh_9.718Na_4.35/SiO₂.
Evaluate catalyst performance using a high pressure parallel fixed bed reactor (PFBR) (PFBR System P/N;132088 from Symyx™ Technologies Inc) , a modular reactor composed of three bays, each of which contains 16 reactor tubes. The tubes in each bay are enclosed in a stainless steel bell jar capable of being pressurized with nitrogen (N₂) at the same pressure as that used in each reaction. Load reactor tubes with 200 microliters (μL) of catalyst, reduce the catalyst in situ at 35 bar (3.5 MPa) for three hours at 350° C. (heating rate of 5° C. per minute) using a gaseous mixture of 90 volume % (vol %) hydrogen (H₂) and 10 vol % N₂, each vol % being based on total gaseous mixture volume. Cool the catalyst to 280° C.
Test the catalyst at a pressure of 35 bar (3.5 MPa) and temperatures of 280° C., 300° C. and 320° C. using a feed mixture of 42.6 vol % H₂, 42.6 vol % CO, 4.8 vol % ethylene and 10 vol % N₂, each vol % being based on total feed mixture volume, flowing over the catalyst at a rate of 20.8 ml/minute. Maintain the temperature at 320° C., but increase the pressure to 90 bars (9 MPa) to evaluate a higher pressure. Increase the temperature to 340° C., but return the pressure to 35 bars (3.5 MPa) to evaluate a higher temperature. Evaluate reactor tube effluent using a Siemens process GC. Replicate this catalyst test cycle two additional times and report test results as an average of three test cycles in Table 1 below.

CEx B

Replicate CEx A, but substitute an aqueous solution (1 ml) that contains 23.18 μmol (3.94 mg) AgNO₃and 19.11 μmol (5.68 mg) Zn(NO₃)₂·6 H₂O for the aqueous solution that contains RhCl₃·3H₂O. The catalyst is represented as Ag_4.635-Zn_3.823-Na_4.35/SiO₂.

CEx C

Replicate CEx A with changes. First, impregnate the silica with an aqueous solution (1 ml) that contains 23.18 μmol (3.94 mg) AgNO₃and dry it overnight at 120° C. Second, impregnate the dried, impregnated silica with 0.475 ml of an aqueous solution that contains 48.59 μmol (10.17 mg) of RhCl₃·3 H₂O and dry it at 100° C. for 4 hrs. Third, impregnate the dried, twice impregnated silica with 0.475 ml of an aqueous solution that contains 21.75 μmol (1.27 mg) of NaCl to form a paste. Subject the paste to drying first under vacuum at 80° C. for 4 hours (hr) and then at 120° C. at atmospheric pressure for 4 hr. Calcine the dried paste as in CEx A to yield a catalyst represented as Rh_9.718-Ag_4.635-Na_4.35/SiO₂.

Ex 1

Replicate CEx C, but add 8.44 μmol (1.6 mg) of tin chloride (SnCl₂) to the aqueous solution that contains NaCl, to yield a catalyst represented as Rh_9.718-Ag_4.635-Sn_2.106Na_4.35/SiO₂.

Ex 2

Replicate Ex 1, but reduce the amount of SnCl₂to 4.22 μmol (0.8 mg) and add 19.11μmol (5.68 mg) of zinc nitrate hexahydrate (Zn(NO₃)₂·6 H₂O) to the aqueous solution that contains AgNO₃to yield a catalyst represented as Rh_9.718-Ag_4.635-Zn_3.823Sn_0.842Na_4.349/SiO₂.

Ex 3

Replicate Ex 1, but add 51.43 μmol (13.19 mg) of magnesium nitrate hexahydrate Mg(NO₃)₂·6 H₂O to the aqueous solution that contains AgNO₃to yield a catalyst represented as Rh_9.718-Ag_4.635-Zn_3.823Mg_10.286Sn_0.842Na_4.349/SiO₂.

Ex 4

Replicate Ex 3 with changes. First, increase the amount of AgNO₃to 34.77 μmol (5.91 mg). Second, increase the amount of Zn(NO₃)₂·6 H₂O to 38.22 μmol (11.37 mg). Represent the catalyst as Rh_9.718-Ag_6.953-Zn_7.646-Mg_10.286-Sn_0.842-Na_4.349/SiO₂. See Table 2 for test results.

Ex 5

Replicate Ex 4, but increase the amount of RhCl₃·3H₂O to 121.475 μmol (24.42 mg). The catalyst is represented as Rh_24.294-Ag_6.953-Zn_7.646-Mg_10.286-Sn_0.842-Na_4.349/SiO₂.

Ex 6

Replicate Ex 5 with changes. First, eliminate addition of the Mg(NO₃)₂·6H₂O. Second, after calcination, use a mortar and pestle to physically mix 502 mg of calcined, dried paste with 1.1 mg of sodium carbonate (Na₂CO₃). The physically mixed catalyst is represented as Rh_2.5-Ag_6.953-Zn_7.646-Sn_0.842-Na_4.349-NC_4.717/SiO₂. “NC” refers to sodium carbonate.

Ex 7

In a single neck glass reactor equipped with a stirring bar add aqueous solutions containing 0.0512 g RhCl₃·3H₂O, 0.0076 g SnCl₂·2 H₂O, 0.0157g AgNO₃and 0.0289 g of Fe(NO₃)₃·9H₂O to 2.0 g of SiO₂support (Aerosil™ 300, Degussa, surface area=300±30 square meters per gram (m²/g)) with constant stirring at room temperature (nominally 25° C.) for an hour. Raise the temperature and evaporate the contents of the reactor to dryness. Dry and calcine the evaporated powder as in CEx A to yield a silica-supported Rh catalyst represented as Rh_9.718Sn_1.685Ag_4.635Fe_3.581/SiO₂. See Table 3 for test results.

Ex 8

Replicate Ex 7 but replace the Fe(NO₃)₃·9H₂O with 0.013 g of Mn(NO₂)₂to yield a catalyst represented as Rh_9.718Sn_1.685Ag_4.635Mn_3.64/SiO₂.

Ex 9

Replicate Ex 7 but replace the Fe(NO₃)₃·9H₂O with 0.0308 g of Cr(NO₃)·9H₂O to yield a catalyst is represented as Rh_9.718Sn_1.685Ag_4.635Cr_3.846/SiO₂.

Ex 10

Replicate Ex 7 but replace the Fe(NO₃)₃·9H₂O with 0.0198 g of Co(NO₃)₂·6H₂O to yield a catalyst represented as Rh_9.718Sn_1.685Ag_4.635Co_3.394/SiO₂.

Ex 11

Replicate Ex 7 but replace the Fe(NO₃)₃·9 H₂O with 0.0070 g of IrCl₄·x H₂O to yield a catalyst represented as Rh_9.718Sn_1.685Ag_4.635Ir_1.04/SiO₂.

TABLE 1

	Temper-	X(eth-	S(Propanal +	S(Eth-
Ex.	ature,	ylene),	Propanol),	ane),
No.	C	%	%	%

D	300	10.2	49.8	46.2
E	300	0.4	7.7	92.3
F	300	4.5	39.2	54.4
1	300	6.5	39.4	58.6
2	300	17.5	53.6	46.1
3	300	19.4	59.6	39.4
D	320	12.2	47.9	45.8
E	320	0.7	19.1	80.9
F	320	8.8	40.3	53.7
1	320	10.5	34.6	61.3
2	320	30.7	50.1	48.0
3	320	33.9	56.6	41.7
D	340	21.9	40.9	46.6
E	340	0.1	27.6	72.4
F	340	44.6	26.8	67.0
1	340	11.2	29.3	63.0
2	340	44.6	49.1	49.1
3	340	53.2	54.4	44.2

X* means conversion;
S** means selectivity

TABLE 2

	Temper-	Pres-	X(eth-	S(Propanal +	S(Eth-
Ex.	ature,	sure,	ylene),	Propanol),	ane),
No.	C	bar	%	%	%

4	280	35	8.8	56.1	43.9
4	300	35	17.1	53.8	45.7
4	320	35	28.4	47.7	50.9
4	320	90	43.0	60.7	37.9
4	340	35	47.3	45.9	52.9
5	300	35	26.9	50.7	48.2
5	320	35	49.5	47.2	50.9
5	340	35	86.8	45.8	52.4
6	300	35	16.7	46.8	53.2
6	320	35	28.5	44.6	55.0
6	340	35	46.4	46.1	50.8

X* means conversion;
S** means selectivity.

TABLE 3

	Temper-	Pres-	X(eth-	S(Propanal +	S(Eth-
Ex.	ature,	sure,	ylene),	Propanol),	ane),
No.	C	bar	%	%	%

7	280	35	61.1	20.7	50.5
8	280	35	79.6	22.9	41.2
9	280	35	70.9	22.2	42.7
10	280	35	63.5	14.7	49.3
11	280	35	58.3	39.4	5.1

X* means conversion;
S** means selectivity, GHSV = 6730 h⁻¹.

The data in Tables 1-3 demonstrate that catalyst compositions comprising, consisting essentially of or consisting of Rh, Ag and Sn show efficient for conversion of a feed that contains ethylene, carbon monoxide and hydrogen to produce at least C3 oxygenates. The data also show that catalyst performance improves when the catalyst further comprises one or more additional elements selected from a group consisting of Zn, alkali metals, alkaline earth metals, and transition metals. Preferred transition metals include iron, manganese, chromium, cobalt and iridium.

Claims

1. A process for converting a feedstream comprising syngas and ethylene to a product stream that comprises at least one three carbon oxygenate, which process comprises placing the feedstream in contact with a heterogeneous catalyst under conditions sufficient to effect conversion of the feedstream to the product stream, the catalyst comprising a combination of metals on a catalyst support, the combination of metals being represented by general formula Rh_aAg_bSn_cX_dY_eO_xwherein X is at least one transition element other than rhodium or silver, Y is at least one element selected from alkali metals and alkaline earth metals, a is a real number within a range of from 0.1 millimole/hectogram to 50 millimole/hectogram, b is a real number within a range of from 0 1 millimole/hectogram to 50 millimole/hectogram, c is a real number within a range of from 0 1 millimole/hectogram to 50 millimole/hectogram, d is a real number within a range of from 0 millimole/hectogram to 250 millimole/hectogram, e is a real number within a range of from 0 millimole/hectogram to 1500 millimole/hectogram, and x is a real number greater than zero needed to balance the total charges of Rh, Ag, Sn, X and Y elements, the catalyst support being at least one of silica, alumina, titania, magnesia, magnesium aluminate, and zinc aluminate.

2. The process of claim 1, wherein X is at least one element selected from a group consisting of zinc, iron, manganese, chromium, cobalt and iridium.

3. The process of claim 1, wherein the conditions include at least one of a temperature within a range of from 100° C. TO 450° C., a pressure within a range of from 12 pounds per square inch gauge (psig) (82.7 kilopascals (KPa)) to 4,000 psig (27.6 megapascals (MPa)), a gas hourly space velocity (GHSV) within a range of from 25 reciprocal hours (h⁻¹) to 25,000 h⁻¹, and a feedstream ratio of ethylene to carbon monoxide to hydrogen (C₂H₄:CO:H₂) within a range of from 0.01:10:10 to 10.0:0.01:0.01.